Widespread blunting of hypothalamic and amygdala-septal activity and behavior in rats with long-term hyperglycemia

• Published in: Behavioural brain research Vol. 310; pp. 59 - 67
• Main Authors: Moreno-Cortés, M.L., Gutiérrez-García, A.G., Guillén-Ruiz, G., Romo-González, T., Contreras, C.M.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.09.2016
• Subjects: Alloxan; Amygdala - metabolism; Amygdala - pathology; Amygdala-septal area; Anhedonia; Animals; Anxiety; Chronic Disease; Diabetes; Dietary Sucrose; Disease Models, Animal; Fos; Hyperglycemia - metabolism; Hyperglycemia - pathology; Hyperglycemia - psychology; Hypothalamus - metabolism; Hypothalamus - pathology; Immunohistochemistry; Ketosis - metabolism; Ketosis - pathology; Ketosis - psychology; Male; Motor Activity - physiology; Orexinergic system; Orexins - metabolism; Proto-Oncogene Proteins c-fos - metabolism; Rats, Wistar; Septum of Brain - metabolism; Septum of Brain - pathology; Anhedonia; Anxiety; Diabetes; Fos; Amygdala-septal area; Orexinergic system
• ISSN: 0166-4328; 1872-7549
• DOI: 10.1016/j.bbr.2016.05.013

•Glucose levels of ∼500mg/dl reduced orexin activity in hypothalamic areas.•Blunted Fos immunoreactivity was detected in amygdala and lateral septal nucleus.•No indicators of anxiety or anhedonia were detected in behavioral tests.•Decreased general locomotion was observed in the open field test.•Long-term hyperglycemia decreased neural activity rather than anxiety or anhedonia. Anxiety and depression in diabetic patients contributes to a poor prognosis, but possible causal relationships have been controversial. Anxiety, fear, and anhedonia are mediated by interactions between different deep structures of the temporal lobe (e.g., amygdala complex and hippocampus) and other forebrain-related structures (e.g., lateral septal nucleus). Connections between these structures and the hypothalamic orexinergic system are necessary for the maintenance of energy and wakefulness. However, few studies have explored the impact of long-term hyperglycemia in these structures on anxiety. We induced long-term hyperglycemia (glucose levels of ∼500mg/dl) in Wistar rats by injecting them with alloxan and simultaneously protecting them from hyperglycemia by injecting them daily with a low dose of insulin (i.e., just enough insulin to avoid death), thus maintaining hyperglycemia and ketonuria for as long as 6 weeks. Compared with controls, long-term hyperglycemic rats exhibited a significant reduction of Fos expression in the lateral septal nucleus and basolateral amygdala, but no differences were found in cerebellar regions. Orexin-A cells appeared to be inactive in the lateral hypothalamus. No differences were found in sucrose consumption or behavior in the elevated plus maze compared with the control group, but a decrease in general locomotion was observed. These data indicate a generalized blunting of the metabolic brain response, accompanied by a decrease in locomotion but no changes in hedonic- or anxiety-like behavior.